FDA UDI In Commercial Distribution 🇺🇸 United States

Endo-Kerrison Shaft

DI: 04250337120261 · Model: EKS15554090 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Endo-Kerrison Shaft
Primary DI
04250337120261
Version / Model
EKS15554090
Catalog Number
EKS15554090
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-29
Public Version
1
Public Version Date
2023-10-09
Public Version Status
New
Public Device Record Key
4e58fa60-e109-4cce-96e4-99ec32819447

Device Description

Endo-Kerrison Shaft

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LRY Punch, Surgical

GMDN Terms

Code Name
35732 Rigid endoscopic biopsy forceps, reusable

Identifiers

Type ID
Primary 04250337120261

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify WL 150 mm / OD 5.5 mm / F 4.0 mm / 90°